Nabumetone
- Product NDC
- 63187-378
- 11-digit product format
- 631870378
- Labeler code
- 63187
- Product ID
- 63187-378_01dcf18d-4211-409a-a0b1-bfa2856ba8b4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nabumetone
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA078671
- Marketing category
- ANDA
- Marketing start
- 2008-03-01
- Marketing end
- 0000-00-00
- Substance
- NABUMETONE
- Active strength
- 750 mg/1
- Pharmacologic classes
- Cyclooxygenase Inhibitors [MoA],Anti-Inflammatory Agents, Non-Steroidal [CS],Nonsteroidal Anti-inflammatory Drug [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63187-378 | NABUMETONE TABLET, FILM COATED [PROFICIENT RX LP] | 3 | Legacy NDC | 20210115_4803746e-3105-423e-b8c6-3735718798e0.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63187-378-30 | 63187037830 | 30 TABLET, FILM COATED in 1 BOTTLE (63187-378-30) | 2016-09-01 | 0000-00-00 | No | No | Current |
| 63187-378-60 | 63187037860 | 60 TABLET, FILM COATED in 1 BOTTLE (63187-378-60) | 2016-09-01 | 0000-00-00 | No | No | Current |
| 63187-378-90 | 63187037890 | 90 TABLET, FILM COATED in 1 BOTTLE (63187-378-90) | 2016-09-01 | 0000-00-00 | No | No | Current |